Description
The ALS Support Group is for patient and families. It is a peer group where people can share their tips for living with ALS and discuss coping strategies.
Meets monthly on the 3rd Monday of the month from 2pm to 3pm EST through Zoom.
Contact: Neuroscience Social Work at 904-953-0332 to be added to the group.
How do I join this group? I am registered with Mayo Connect.
Thank you.
Pat Clark
Hi I am in Canada and diagnosed with Bulbar Palsy ALS March 2023. I cannot speak, but have app to communicate. My biggest frustration is drooling, trying to get under control without having mouth too dry. I have tried drops and a prescribed mouth rinse with not much difference. What is recommended that has worked for PALS.? It really stops me from socializing.
My son-in-law has same problem. We fold a paper towel multiple times and place it on his mouth (needs to be changed frequently but it works).
Update on previous post you may have to double the paper towels.
Me as well